合計: 4 |
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PMID (PMCID) | ||
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30305036 (6180649) |
OTHER | |
Sickle cell disease: a case report of renal amyloidosis. | ||
Bugeja A, Blanco P, Clark EG, Sood MM. BMC Nephrol. 2018;19(1):256. |
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The development of proteinuria and reduced glomerular filtration rate is associated with higher mortality among patients with sickle cell disease (SCD). | ||
25035790 |
OTHER | |
A novel case report of sickle cell disease-associated immunoglobulin A nephropathy: the diagnostic value of erythrocyte dysmorphism evaluation. | ||
Silva GE, Teixeira AC, Vergna JG, Salgado-Filho N, Crivellentti LZ, Costa RS, Dantas M. Int J Clin Exp Med. 2014;7(6):1619-22. |
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This case report describes a novel case of a patient with sickle cell disease who presented with proteinuria and microscopic dysmorphic (glomerular) hematuria. | ||
15704213 |
MIXED_SAMPLE | Child |
Enalapril and hydroxyurea therapy for children with sickle nephropathy. | ||
Fitzhugh CD, Wigfall DR, Ware RE. Pediatr Blood Cancer. 2005;45(7):982-5. |
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Proteinuria in children with sickle cell anemia (SCA) is an early sign of sickle nephropathy, and portends the development of nephrotic syndrome and chronic renal failure. | ||
7637482 |
MIXED_SAMPLE | Child |
Glomerulonephritis after human parvovirus infection in homozygous sickle-cell disease. | ||
Wierenga KJ, Pattison JR, Brink N, Griffiths M, Miller M, Shah DJ, Williams W, Serjeant BE, Serjeant GR. Lancet. 1995;346(8973):475-6. |
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Glomerulonephritis with proteinuria of sufficient degree to manifest the nephrotic syndrome followed aplastic crises induced by human parvovirus (B19) in seven patients with homozygous sickle-cell disease, within 7 days in five patients and 6-7 weeks in two. |